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397261

Sigma-Aldrich

N-(2-Aminoethyl)acetamide

technical grade, 90%

Synonym(s):

N-Acetylethylenediamine

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About This Item

Linear Formula:
CH3C(O)NHCH2CH2NH2
CAS Number:
1001-53-2
Molecular Weight:
102.14
Beilstein:
1743120
MDL number:
MFCD00008163
UNSPSC Code:
12352100
PubChem Substance ID:
24864696
NACRES:
NA.22

grade

technical grade

Assay

90%

refractive index

n20/D 1.485 (lit.)

bp

128 °C/3 mmHg (lit.)

mp

50 °C (lit.)

density

1.066 g/mL at 25 °C (lit.)

SMILES string

CC(=O)NCCN

InChI

1S/C4H10N2O/c1-4(7)6-3-2-5/h2-3,5H2,1H3,(H,6,7)

InChI key

DAKZISABEDGGSV-UHFFFAOYSA-N

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General description

N-(2-Aminoethyl)acetamide is an organic building block.

Application

N-(2-Aminoethyl)acetamide may be used in the preparation of mixed two-component monolayers on glassy carbon. It may be used in the synthesis of lysidine.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

>230.0 °F - closed cup

Flash Point(C)

> 110 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
0000237956
0000231494
BGBB8824
BGBB0272V
BGBB0272

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Dalton transactions (Cambridge, England : 2003), 45(40), 15931-15941 (2016-07-08)
A new long-tethered boron-containing (P-B-P)-pincer ligand 8 has been synthesized. Complexation of 8 with [Ir(coe)
Yoonkyung Kim et al.
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As a continued effort to develop multivalent ligands to enhance the pharmacological effects of monomeric drugs, DITC-APEC, a chemically reactive nucleoside A(2A) adenosine receptor (AR) agonist, was employed to derivatize the surface of third-generation (G3) polyamidoamine (PAMAM) dendrimers. The resulting
The Mechanism of Acid Hydrolysis of Lysidine and N-(2-Aminotheyl) acetamide and Related Amides.
Haake P and Watson J.
The Journal of Organic Chemistry, 35(12), 4063-4067 (1970)
Emma J Wright et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 20(19), 5550-5554 (2014-04-12)
Mixed two-component monolayers on glassy carbon are prepared by electrochemical oxidation of N-(2-aminoethyl)acetamide and mono-N-Boc-hexamethylenediamine in mixed solution. Subsequent N-deprotection, amide coupling and solid-phase synthetic steps lead to electrode-surface functionalisation with maleimide, with controlled partial coverage of this cysteine-binding group
Ling Li et al.
Molecular cell, 80(3), 525-540 (2020-10-18)
Well-balanced and timed metabolism is essential for making a high-quality egg. However, the metabolic framework that supports oocyte development remains poorly understood. Here, we obtained the temporal metabolome profiles of mouse oocytes during in vivo maturation by isolating large number of

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